Furosemide

Product NDC
70860-302
11-digit product format
708600302
Labeler code
70860
Product ID
70860-302_31f81122-35a2-44aa-89a8-251cd0afa9f0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Athenex Pharmaceutical Division, LLC.
Application
ANDA214766
Marketing category
ANDA
Marketing start
2021-03-15
Marketing end
0000-00-00
Substance
FUROSEMIDE
Active strength
10 mg/mL
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70860-302-02ML - Milliliter70860-302f292509c-22f9-44b7-a10a-eb2b1a0d220412021-11-09
70860-302-04ML - Milliliter70860-30209849fea-6774-48ec-b985-208496debe7212021-11-09
70860-302-10ML - Milliliter70860-302f898a7a6-c2c1-46e8-8378-4ea021b1f09512021-11-09
70860-302-41ML - Milliliter70860-3020f27d46a-66a9-4666-956c-65196896a58312021-11-09
70860-302-42ML - Milliliter70860-3029c4ef7eb-7ead-450f-9b1d-5a700463cd2812021-11-09
70860-302-43ML - Milliliter70860-30208a02748-082d-4745-b189-ddef3d173deb12021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70860-302-027086003020225 VIAL, SINGLE-DOSE in 1 CARTON (70860-302-02) > 2 mL in 1 VIAL, SINGLE-DOSE (70860-302-41) 2021-03-150000-00-00NoNoCurrent
70860-302-047086003020425 VIAL, SINGLE-DOSE in 1 CARTON (70860-302-04) > 4 mL in 1 VIAL, SINGLE-DOSE (70860-302-42) 2021-03-150000-00-00NoNoCurrent
70860-302-107086003021025 VIAL, SINGLE-DOSE in 1 CARTON (70860-302-10) > 10 mL in 1 VIAL, SINGLE-DOSE (70860-302-43) 2021-03-150000-00-00NoNoCurrent